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Volumn 42, Issue 11, 2002, Pages 1069-1072

Differential diagnosis of spinocerebellar ataxia

Author keywords

Anticipation; Diagnostic criteria; Differential diagnosis; Spinocerebellar ataxia; Triplet repeat disorder

Indexed keywords

AUTONOMIC DYSFUNCTION; CEREBELLAR ATAXIA; CONFERENCE PAPER; CORRELATION ANALYSIS; DENTATORUBROPALLIDOLUYSIAN ATROPHY; DIFFERENTIAL DIAGNOSIS; DISEASE SEVERITY; DYSAUTONOMIA; HUMAN; JAPAN; MACHADO JOSEPH DISEASE; ONSET AGE; PARKINSONISM; PHENOTYPE; SPINOCEREBELLAR DEGENERATION; TRINUCLEOTIDE REPEAT; VERTIGO;

EID: 0037610930     PISSN: 0009918X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Conference Paper
Times cited : (2)

References (10)
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  • 3
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    • Sasaki H, Fukazawa T, Wakisaka A, et al: Central phenotype and related varieties of spinocerebellar ataxia 2 (SCA2) - a clinical and genetic study with a pedigree in the Japanese. J Neurol Sci 144: 176-181, 1996
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  • 5
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    • Klockgether T, Schöls L, Abele M, et al: Age related axonal neuropathy in spinocerebellar ataxia type 3/ Machado-Joseph disease (SCA3/MJD). J Neurol Neurosurg Psychiatry 66: 222-224, 1999
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  • 6
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  • 7
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  • 9
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  • 10
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    • Consensus statement on the diagnosis of multiple system atrophy
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.